Search genes and transcripts, design primers, and store and share the results with your lab — all in one workspace.
What you can do
Oligomics brings gene search, primer design, and protocol storage into a single workspace built around how molecular biology labs actually work.
Look up any gene and see every transcript variant pulled directly from NCBI — accession numbers, biotypes, validation status, and length, all in one view.
Jump straight from a transcript to primer design, with results saved back against the gene so you can find them again later.
Keep your primers and protocols in one place instead of scattered across spreadsheets, lab notebooks, and old emails.
Add colleagues as friends and share primers with them directly, so a working primer only has to be found once per lab.
Why Oligomics
Most labs manage primers and protocols across a patchwork of spreadsheets, shared drives, and lab notebooks. Good primers get redesigned from scratch because nobody remembers they already exist. Oligomics fixes that by giving every researcher a single, searchable workspace.
Because gene and transcript data comes straight from NCBI and primer results are stored alongside PCR and gel outcomes, your library gets more useful — and more trustworthy — with every experiment you log.
Search your lab's shared library before starting a new design — if it's been done before, it's already there.
Transcript and accession data is sourced directly from NCBI, so you're always designing against current records.
Log PCR and gel outcomes against each primer so your library reflects what actually works at the bench.
Every primer can be shared with colleagues, so knowledge stays with the lab rather than one person's laptop.
From gene to bench, in four steps
Search a gene
Find it and browse every transcript variant
Design primers
Generate primers directly from the transcript
Log results
Record PCR and gel outcomes against each primer
Share with your lab
Add friends and pass on what worked
See it in action
Every transcript for a gene, aligned on one scale — so exon differences, retained introns, and UTR length are obvious before you design a single primer.
Search genes, design primers, and keep protocols in one shared place your whole team can trust.
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